Carboxylic acid: Difference between revisions
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Carboxylic acids contain a carbon atom that is attached to one oxygen atom with a double bond, a [[hydroxyl group]] by a single bond, and one additional bond to an organic group (R-) which is often an [[alkane]] or [[alkene]] group. They are often written as R-C(=O)OH, , R-COOH or R-CO<sub>2</sub>H. Carboxylic acids are weak [[Brønsted-Lowry acid-base theory|Brønsted-Lowry]] acids which only partially dissociate in water to produce the [[hydronium ion]] [H<sub>3</sub>O]<sup>+</sup> and the conjugate base of the acid, [R-CO<sub>2</sub>]<sup>-</sup>. Although small carboxylic acids are soluble in water, larger acids are increasingly insoluble in water but increasingly soluble in non-polar solvents. | Carboxylic acids contain a carbon atom that is attached to one oxygen atom with a double bond, a [[hydroxyl group]] by a single bond, and one additional bond to an organic group (R-) which is often an [[alkane]] or [[alkene]] group. They are often written as R-C(=O)OH, , R-COOH or R-CO<sub>2</sub>H. Carboxylic acids are weak [[Brønsted-Lowry acid-base theory|Brønsted-Lowry]] acids which only partially dissociate in water to produce the [[hydronium ion]] [H<sub>3</sub>O]<sup>+</sup> and the conjugate base of the acid, [R-CO<sub>2</sub>]<sup>-</sup>. Although small carboxylic acids are soluble in water, larger acids are increasingly insoluble in water but increasingly soluble in non-polar solvents. | ||
== | == Stability of the conjugate base == | ||
The negative charge of the conjugate base is shared between the two electronegative oxygen atoms, and this effect can be visualized as two different resonance structures. The strength of carboxylic acids is effected by the organic group to which it is attached. If the R-group is an electron acceptor, it can stabilize the negative charge of the conjugate base either through inductive or resonance effects and therefore increase the acid strength. | The negative charge of the conjugate base is shared between the two electronegative oxygen atoms, and this effect can be visualized as two different resonance structures. The strength of carboxylic acids is effected by the organic group to which it is attached. If the R-group is an electron acceptor, it can stabilize the negative charge of the conjugate base either through inductive or resonance effects and therefore increase the acid strength. | ||
== | == Chemical reactions == | ||
Carboxylic acids can be formed by the hydrolysis of a corresponding [[ester]] or [[amide]]. Thus, [[ethyl acetate]] can be hydrolyzed to form acetic acid and ethanol. Conversely, the [[Fisher esterification]] reaction can be used to react a carboxylic acid with an alcohol to form an ester. Carboxylic acids can also be reduced to form aldehydes or further reduced to form primary alcohols. | Carboxylic acids can be formed by the hydrolysis of a corresponding [[ester]] or [[amide]]. Thus, [[ethyl acetate]] can be hydrolyzed to form acetic acid and ethanol. Conversely, the [[Fisher esterification]] reaction can be used to react a carboxylic acid with an alcohol to form an ester. Carboxylic acids can also be reduced to form aldehydes or further reduced to form primary alcohols. | ||
== | == Flavoring agents == | ||
Their tart taste makes many carboxylic acids useful as flavoring agents in the food industry. Citric acid is widely used in fruit punches and candy. | Their tart taste makes many carboxylic acids useful as flavoring agents in the food industry. Citric acid is widely used in fruit punches and candy. | ||
==References== | ==References== | ||
{{reflist}} | |||
Revision as of 19:25, 19 February 2010
Carboxylic acids are important precursor chemicals both in the lab and in living organisms. The twenty common amino acids are a particularly important class of carboxylic acids. Carboxylic acids are generally tart in taste and are thus widely used in the food industry. Foods are often preserved with the addition of sodium benzoate, which is the conjugate base of benzoic acid. Acetic acid is a carboxylic acid that gives vinegar its bite. Formic acid has historically been used to preserve specimens of animal tissue.
chemical properties
Carboxylic acids contain a carbon atom that is attached to one oxygen atom with a double bond, a hydroxyl group by a single bond, and one additional bond to an organic group (R-) which is often an alkane or alkene group. They are often written as R-C(=O)OH, , R-COOH or R-CO2H. Carboxylic acids are weak Brønsted-Lowry acids which only partially dissociate in water to produce the hydronium ion [H3O]+ and the conjugate base of the acid, [R-CO2]-. Although small carboxylic acids are soluble in water, larger acids are increasingly insoluble in water but increasingly soluble in non-polar solvents.
Stability of the conjugate base
The negative charge of the conjugate base is shared between the two electronegative oxygen atoms, and this effect can be visualized as two different resonance structures. The strength of carboxylic acids is effected by the organic group to which it is attached. If the R-group is an electron acceptor, it can stabilize the negative charge of the conjugate base either through inductive or resonance effects and therefore increase the acid strength.
Chemical reactions
Carboxylic acids can be formed by the hydrolysis of a corresponding ester or amide. Thus, ethyl acetate can be hydrolyzed to form acetic acid and ethanol. Conversely, the Fisher esterification reaction can be used to react a carboxylic acid with an alcohol to form an ester. Carboxylic acids can also be reduced to form aldehydes or further reduced to form primary alcohols.
Flavoring agents
Their tart taste makes many carboxylic acids useful as flavoring agents in the food industry. Citric acid is widely used in fruit punches and candy.